Variant report

Variant	nsv890336
Chromosome Location	chr8:8396676-8500562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2147)
CpG islands
(count:549)
Chromatin interactive
region (count:53)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2147 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8458475-8458706	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8441372-8441831	HepG2	liver:	n/a	n/a
3	ATF2	chr8:8472832-8473524	GM12878	blood:	n/a	n/a
4	ATF2	chr8:8483190-8484656	GM12878	blood:	n/a	n/a
5	ATF2	chr8:8483666-8484639	GM12878	blood:	n/a	n/a
6	ATF2	chr8:8475296-8476633	GM12878	blood:	n/a	n/a
7	ATF2	chr8:8402416-8402973	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:8426361-8427059	GM12878	blood:	n/a	n/a
9	ATF2	chr8:8497843-8499427	GM12878	blood:	n/a	n/a
10	ATF2	chr8:8497895-8499479	GM12878	blood:	n/a	n/a
11	ATF2	chr8:8475053-8476298	GM12878	blood:	n/a	n/a
12	ATF2	chr8:8407452-8407867	GM12878	blood:	n/a	n/a
13	ATF2	chr8:8426436-8427026	GM12878	blood:	n/a	n/a
14	ATF2	chr8:8472786-8473622	GM12878	blood:	n/a	n/a
15	ATF2	chr8:8489238-8489950	GM12878	blood:	n/a	n/a
16	ATF3	chr8:8500553-8501169	A549	lung:	n/a	n/a
17	ATF3	chr8:8458075-8458736	A549	lung:	n/a	n/a
18	ATF3	chr8:8468794-8469337	A549	lung:	n/a	chr8:8468872-8468885
19	ATF3	chr8:8458176-8458817	A549	lung:	n/a	n/a
20	BACH1	chr8:8422093-8422283	H1-hESC	embryonic stem cell:	n/a	chr8:8422188-8422202
21	BACH1	chr8:8402290-8402821	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr8:8472961-8473306	GM12878	blood:	n/a	n/a
23	BATF	chr8:8498646-8499449	GM12878	blood:	n/a	n/a
24	BATF	chr8:8475598-8475911	GM12878	blood:	n/a	n/a
25	BATF	chr8:8498669-8499449	GM12878	blood:	n/a	n/a
26	BATF	chr8:8472929-8473340	GM12878	blood:	n/a	n/a
27	BATF	chr8:8475404-8475994	GM12878	blood:	n/a	n/a
28	BATF	chr8:8426529-8426975	GM12878	blood:	n/a	n/a
29	BATF	chr8:8426530-8427011	GM12878	blood:	n/a	n/a
30	BATF	chr8:8483272-8483718	GM12878	blood:	n/a	n/a
31	BATF	chr8:8407590-8407858	GM12878	blood:	n/a	n/a
32	BATF	chr8:8483243-8483498	GM12878	blood:	n/a	n/a
33	BATF	chr8:8407563-8407870	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:8498662-8499400	GM12878	blood:	n/a	chr8:8499252-8499261 chr8:8498878-8498887 chr8:8498700-8498709
35	BCL11A	chr8:8483248-8483645	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:8483928-8484299	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:8472862-8473359	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:8426517-8426963	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
39	BCL11A	chr8:8472917-8473272	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:8498698-8499350	GM12878	blood:	n/a	chr8:8499252-8499261 chr8:8498878-8498887 chr8:8498700-8498709
41	BCL11A	chr8:8483232-8483584	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:8483923-8484155	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:8426505-8426978	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
44	BCL11A	chr8:8475612-8476007	GM12878	blood:	n/a	n/a
45	BCL3	chr8:8475163-8475540	GM12878	blood:	n/a	n/a
46	BCL3	chr8:8500356-8501131	A549	lung:	n/a	n/a
47	BCL3	chr8:8475563-8476117	GM12878	blood:	n/a	n/a
48	BCL3	chr8:8483277-8483780	GM12878	blood:	n/a	n/a
49	BCL3	chr8:8468642-8469393	A549	lung:	n/a	n/a
50	BCL3	chr8:8472921-8473384	GM12878	blood:	n/a	chr8:8473353-8473361

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8493391-8493441	SKMC	muscle:	n/a
2	chr8:8419587-8419637	HAEpiC	amniotic membrane:	n/a
3	chr8:8419587-8419637	AG09319	gingival:	n/a
4	chr8:8420735-8420785	PrEC	prostate:	n/a
5	chr8:8419587-8419637	GM12892	blood:	n/a
6	chr8:8493391-8493441	RPTEC	kidney:	n/a
7	chr8:8412440-8412490	MCF-7	breast:	n/a
8	chr8:8469173-8469223	LNCaP	prostate:	n/a
9	chr8:8420735-8420785	HCF	heart:	n/a
10	chr8:8474738-8474788	HIPEpiC	eye:	n/a
11	chr8:8420735-8420785	H1-hESC	embryonic stem cell:	embryo
12	chr8:8439596-8439646	HCF	heart:	n/a
13	chr8:8419587-8419637	SK-N-MC	brain:	n/a
14	chr8:8402366-8402416	PrEC	prostate:	n/a
15	chr8:8474738-8474788	SAEC	small airway:	n/a
16	chr8:8483549-8483599	HRE	kidney:	n/a
17	chr8:8483549-8483599	PrEC	prostate:	n/a
18	chr8:8412440-8412490	PrEC	prostate:	n/a
19	chr8:8420735-8420785	HRPEpiC	eye:	n/a
20	chr8:8483549-8483599	NHBE	bronchial:	n/a
21	chr8:8439596-8439646	K562	blood:	n/a
22	chr8:8420735-8420785	Hepatocyte	liver:	n/a
23	chr8:8483549-8483599	PFSK-1	brain:	n/a
24	chr8:8474738-8474788	AG09319	gingival:	n/a
25	chr8:8474738-8474788	HCM	heart:	n/a
26	chr8:8420735-8420785	GM06990	blood:	n/a
27	chr8:8420735-8420785	HUVEC	blood vessel:	n/a
28	chr8:8483549-8483599	HEK293	kidney:	embryo
29	chr8:8439596-8439646	BE2_C	brain:	n/a
30	chr8:8420735-8420785	BJ	skin:	n/a
31	chr8:8439596-8439646	PANC-1	pancreas:	n/a
32	chr8:8483549-8483599	BE2_C	brain:	n/a
33	chr8:8469173-8469223	HRCEpiC	kidney:	n/a
34	chr8:8412440-8412490	HIPEpiC	eye:	n/a
35	chr8:8419587-8419637	ProgFib	skin:	n/a
36	chr8:8420735-8420785	SK-N-SH	brain:	n/a
37	chr8:8493391-8493441	Caco-2	colon:	n/a
38	chr8:8412440-8412490	IMR90	lung:	fetal
39	chr8:8402366-8402416	IMR90	lung:	fetal
40	chr8:8420735-8420785	AG04449	skin:	fetal
41	chr8:8483549-8483599	Hepatocyte	liver:	n/a
42	chr8:8439596-8439646	NHBE	bronchial:	n/a
43	chr8:8469173-8469223	ovcar-3	ovarian:	n/a
44	chr8:8474738-8474788	H1-hESC	embryonic stem cell:	embryo
45	chr8:8439596-8439646	NH-A	brain:	n/a
46	chr8:8439596-8439646	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:8439596-8439646	HRCEpiC	kidney:	n/a
48	chr8:8439596-8439646	NHDF-neo	bronchial:	n/a
49	chr8:8483549-8483599	CMK	blood:	n/a
50	chr8:8412440-8412490	ProgFib	skin:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:8398950..8401316-chr8:8404016..8406720,2	MCF-7	breast:
2	chr8:8411447..8415576-chr8:8419918..8422813,4	MCF-7	breast:
3	chr8:8395182..8397914-chr8:8412349..8414858,2	MCF-7	breast:
4	chr8:8426650..8428995-chr8:8432055..8433956,2	MCF-7	breast:
5	chr8:8243125..8245371-chr8:8446587..8449167,2	MCF-7	breast:
6	chr8:8317642..8319537-chr8:8411427..8414292,2	MCF-7	breast:
7	chr8:8467934..8469639-chr8:8471429..8473013,2	MCF-7	breast:
8	chr8:8424041..8426477-chr8:8428202..8430360,2	K562	blood:
9	chr8:8411664..8414236-chr8:8423427..8425709,2	MCF-7	breast:
10	chr8:8241776..8244765-chr8:8431330..8433692,2	MCF-7	breast:
11	chr8:8402871..8405951-chr8:8409300..8411687,3	MCF-7	breast:
12	chr8:8411406..8413359-chr8:8458313..8460568,2	MCF-7	breast:
13	chr8:8430219..8432230-chr8:8438202..8440679,2	K562	blood:
14	chr8:8405511..8408091-chr8:8411497..8414103,2	MCF-7	breast:
15	chr8:8422238..8425021-chr8:8428768..8430499,2	MCF-7	breast:
16	chr8:8405511..8408091-chr8:8411497..8414103,2	MCF-7	breast:
17	chr8:8422238..8425021-chr8:8428768..8430499,2	MCF-7	breast:
18	chr8:8489853..8492603-chr8:8493260..8496141,2	K562	blood:
19	chr8:8395034..8396944-chr8:8396976..8398934,2	MCF-7	breast:
20	chr8:8422023..8423577-chr8:8457115..8459478,2	MCF-7	breast:
21	chr8:8458941..8461219-chr8:8461272..8463355,2	MCF-7	breast:
22	chr19:2475818..2476408-chr8:8412492..8413168,2	HCT-116	colon:
23	chr8:8403320..8405523-chr8:8412097..8413733,2	K562	blood:
24	chr8:8405670..8408413-chr8:8410858..8412473,2	K562	blood:
25	chr8:8411664..8414236-chr8:8423427..8425709,2	MCF-7	breast:
26	chr8:8463109..8465493-chr8:8467640..8471608,3	MCF-7	breast:
27	chr8:8405670..8408413-chr8:8410858..8412473,2	K562	blood:
28	chr8:8411447..8415576-chr8:8419918..8422813,4	MCF-7	breast:
29	chr8:8431429..8434026-chr8:8436657..8439955,3	MCF-7	breast:
30	chr8:8426650..8428995-chr8:8432055..8433956,2	MCF-7	breast:
31	chr8:8467934..8469639-chr8:8471429..8473013,2	MCF-7	breast:
32	chr8:8458941..8461219-chr8:8461272..8463355,2	MCF-7	breast:
33	chr8:8431429..8434026-chr8:8436657..8439955,3	MCF-7	breast:
34	chr8:8467892..8470018-chr8:8516521..8519296,2	MCF-7	breast:
35	chr8:8395182..8397914-chr8:8412349..8414858,2	MCF-7	breast:
36	chr8:8412630..8415274-chr8:8423101..8424700,2	K562	blood:
37	chr8:8422023..8423577-chr8:8457115..8459478,2	MCF-7	breast:
38	chr8:8467347..8470547-chr8:8493225..8496865,3	MCF-7	breast:
39	chr8:8412630..8415274-chr8:8423101..8424700,2	K562	blood:
40	chr8:8402871..8405951-chr8:8409300..8411687,3	MCF-7	breast:
41	chr8:8411406..8413359-chr8:8458313..8460568,2	MCF-7	breast:
42	chr8:8424041..8426477-chr8:8428202..8430360,2	K562	blood:
43	chr8:8242353..8245621-chr8:8412264..8415410,4	MCF-7	breast:
44	chr8:8484452..8486577-chr8:8508195..8510591,2	MCF-7	breast:
45	chr8:8467347..8470547-chr8:8493225..8496865,3	MCF-7	breast:
46	chr8:8411777..8414467-chr8:8512420..8515459,3	MCF-7	breast:
47	chr8:8403320..8405523-chr8:8412097..8413733,2	K562	blood:
48	chr8:8458349..8461087-chr8:8498187..8500312,2	MCF-7	breast:
49	chr8:8395034..8396944-chr8:8396976..8398934,2	MCF-7	breast:
50	chr8:8398950..8401316-chr8:8404016..8406720,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLDN23-3	chr8:8464107-8464458	l_3541_chr8:8456313-8464458_testes
2	lnc-CLDN23-1	chr8:8418901-8419044	NONHSAT124878
3	lnc-CLDN23-1	chr8:8418904-8419044	ENSG00000253130
4	lnc-CLDN23-1	chr8:8418901-8419044	ENSG00000253130
5	lnc-CLDN23-1	chr8:8421617-8422045	ENSG00000253130
6	lnc-PRAGMIN.1-9	chr8:8439864-8440165	NONHSAT124884
7	lnc-CLDN23-1	chr8:8419343-8419634	NONHSAT124878
8	lnc-CLDN23-1	chr8:8412783-8413276	NONHSAT124878
9	lnc-CLDN23-1	chr8:8418711-8418867	NONHSAT124878
10	lnc-CLDN23-1	chr8:8426697-8427048	XLOC_006698
11	lnc-CLDN23-1	chr8:8422143-8422213	XLOC_006698
12	lnc-CLDN23-1	chr8:8417404-8417553	NONHSAT124878
13	lnc-CLDN23-2	chr8:8419343-8419634	ENSG00000253774
14	lnc-CLDN23-1	chr8:8426474-8428227	NONHSAT124878
15	lnc-CLDN23-1	chr8:8421329-8422570	NONHSAT124878
16	lnc-CLDN23-1	chr8:8426697-8427198	ENSG00000253130
17	lnc-CLDN23-1	chr8:8431228-8435105	NONHSAT124878
18	lnc-CLDN23-2	chr8:8417404-8417553	ENSG00000253774
19	lnc-CLDN23-2	chr8:8418711-8418847	ENSG00000253774
20	lnc-CLDN23-3	chr8:8456314-8456508	l_3541_chr8:8456313-8464458_testes
21	lnc-PRAGMIN.1-4	chr8:8413248-8413598	ENSG00000253343
22	lnc-PRAGMIN.1-4	chr8:8418430-8418475	ENSG00000253343
23	lnc-CLDN23-3	chr8:8459497-8459623	l_3541_chr8:8456313-8464458_testes

No data

Variant related genes	Relation type
ENSG00000264445	TF binding region
ENSG00000253774	TF binding region
ENSG00000253343	TF binding region
RN7SL178P	TF binding region
ENSG00000253130	TF binding region
ENSG00000264445	CpG island
ENSG00000253774	CpG island
ENSG00000253343	CpG island
RN7SL178P	CpG island
ENSG00000253130	CpG island
ENSG00000264445	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions
ENSG00000263616	chromatin interactions
ENSG00000099860	chromatin interactions

Extended variants
information (count: 5833 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:5833 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17153465	chr8:8396676-8396677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564836366	chr8:8396688-8396689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4367542	chr8:8396737-8396738	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs544356085	chr8:8396774-8396775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146515722	chr8:8396777-8396778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529769777	chr8:8396786-8396787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192544121	chr8:8396797-8396798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs118047957	chr8:8396833-8396834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74587063	chr8:8396868-8396869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7005440	chr8:8396886-8396887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs184827267	chr8:8396924-8396925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141052867	chr8:8396937-8396938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371956860	chr8:8396983-8396984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553831004	chr8:8396986-8396987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570561487	chr8:8396995-8396996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532218612	chr8:8396996-8396997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189732137	chr8:8397009-8397010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558439810	chr8:8397016-8397017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575151408	chr8:8397040-8397041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544099337	chr8:8397044-8397045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375256499	chr8:8397049-8397050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554716161	chr8:8397050-8397051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574531146	chr8:8397097-8397098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540352639	chr8:8397102-8397103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560286285	chr8:8397103-8397104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532183974	chr8:8397104-8397105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34696727	chr8:8397146-8397147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545774881	chr8:8397150-8397151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563176918	chr8:8397151-8397152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144734553	chr8:8397153-8397154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4409404	chr8:8397157-8397158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565497854	chr8:8397160-8397161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568669915	chr8:8397169-8397170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527880642	chr8:8397173-8397174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547529153	chr8:8397174-8397175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573346473	chr8:8397205-8397206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371882994	chr8:8397231-8397232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148842357	chr8:8397237-8397238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553297782	chr8:8397256-8397257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181629304	chr8:8397265-8397266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556111476	chr8:8397270-8397271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569074853	chr8:8397281-8397282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375509812	chr8:8397305-8397306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538175957	chr8:8397309-8397310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554547220	chr8:8397320-8397321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534718388	chr8:8397333-8397334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541564813	chr8:8397335-8397336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574620686	chr8:8397351-8397352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143452390	chr8:8397354-8397355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79023698	chr8:8397375-8397376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8389200-8403000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:8395200-8402600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:8395400-8401600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr8:8395800-8401200	Weak transcription	HSMMtube	muscle
5	chr8:8395800-8401600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr8:8396000-8401200	Weak transcription	HUVEC	blood vessel
7	chr8:8396000-8401400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:8396000-8401600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:8396000-8401800	Weak transcription	Placenta	Placenta
10	chr8:8396000-8405000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:8397200-8398200	Enhancers	Stomach Mucosa	stomach
12	chr8:8400400-8404600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:8400600-8402000	Enhancers	Primary B cells from peripheral blood	blood
14	chr8:8400800-8401600	Enhancers	Primary hematopoietic stem cells	blood
15	chr8:8400800-8403400	Enhancers	GM12878-XiMat	blood
16	chr8:8401000-8404400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:8401200-8401600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr8:8401200-8402600	Enhancers	HUVEC	blood vessel
19	chr8:8401200-8403600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:8401200-8403600	Enhancers	HSMMtube	muscle
21	chr8:8401200-8404400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:8401400-8402200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:8401400-8403200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:8401400-8403400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:8401400-8403400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr8:8401400-8403600	Enhancers	Right Atrium	heart
27	chr8:8401400-8404000	Enhancers	Adipose Nuclei	Adipose
28	chr8:8401600-8402200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr8:8401600-8402600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:8401600-8403200	Enhancers	Placenta Amnion	Placenta Amnion
31	chr8:8401600-8403400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:8401600-8403400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr8:8401600-8403400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:8401600-8403600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:8401600-8403600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:8401600-8403600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:8401600-8405800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr8:8401800-8402000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:8401800-8402000	Enhancers	Duodenum Mucosa	Duodenum
40	chr8:8401800-8402200	Enhancers	Left Ventricle	heart
41	chr8:8401800-8403400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr8:8401800-8403400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:8401800-8403400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr8:8401800-8403400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:8401800-8403400	Enhancers	Brain Germinal Matrix	brain
46	chr8:8401800-8403400	Enhancers	Placenta	Placenta
47	chr8:8401800-8403400	Enhancers	Spleen	Spleen
48	chr8:8401800-8403400	Enhancers	A549	lung
49	chr8:8401800-8403400	Enhancers	NH-A	brain
50	chr8:8401800-8403800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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