Variant report

Variant	nsv1022866
Chromosome Location	chr6:167108740-167345629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2751)
CpG islands
(count:5683)
Chromatin interactive
region (count:106)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2751 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167200218-167200546	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167188768-167188974	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
4	ARID3A	chr6:167324658-167325218	K562	blood:	n/a	n/a
5	ATF1	chr6:167328715-167329352	K562	blood:	n/a	n/a
6	ATF1	chr6:167213787-167214099	K562	blood:	n/a	n/a
7	ATF1	chr6:167287376-167287880	K562	blood:	n/a	n/a
8	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
9	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
10	ATF1	chr6:167238143-167238339	K562	blood:	n/a	n/a
11	ATF1	chr6:167324192-167325358	K562	blood:	n/a	n/a
12	ATF1	chr6:167320881-167321225	K562	blood:	n/a	n/a
13	ATF1	chr6:167240077-167240150	K562	blood:	n/a	n/a
14	ATF1	chr6:167190190-167190394	K562	blood:	n/a	n/a
15	ATF1	chr6:167345566-167345627	K562	blood:	n/a	n/a
16	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
17	ATF2	chr6:167243498-167244485	GM12878	blood:	n/a	n/a
18	ATF2	chr6:167320633-167321310	GM12878	blood:	n/a	n/a
19	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
20	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
21	ATF2	chr6:167243583-167244420	GM12878	blood:	n/a	n/a
22	ATF2	chr6:167200233-167200574	GM12878	blood:	n/a	n/a
23	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
24	BACH1	chr6:167198886-167198899	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:167180403-167180549	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:167317880-167318113	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:167196277-167196415	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:167290924-167291004	K562	blood:	n/a	n/a
29	BACH1	chr6:167174931-167175059	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167183960-167184643	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167108688-167108908	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167164829-167164988	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167216081-167216348	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167276270-167276880	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
36	BATF	chr6:167197269-167197664	GM12878	blood:	n/a	n/a
37	BATF	chr6:167247594-167247848	GM12878	blood:	n/a	n/a
38	BATF	chr6:167243631-167244353	GM12878	blood:	n/a	n/a
39	BATF	chr6:167263166-167263351	GM12878	blood:	n/a	n/a
40	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
41	BATF	chr6:167320864-167321175	GM12878	blood:	n/a	n/a
42	BATF	chr6:167197282-167197733	GM12878	blood:	n/a	n/a
43	BATF	chr6:167243652-167243968	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167197224-167197721	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:167243593-167243973	GM12878	blood:	n/a	n/a
46	BCL11A	chr6:167244064-167244380	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:167244040-167244445	GM12878	blood:	n/a	n/a
48	BCL11A	chr6:167243668-167243958	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:167197263-167197805	GM12878	blood:	n/a	n/a
50	BCL3	chr6:167315018-167316313	GM12878	blood:	n/a	n/a

(count:5683 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167276650-167276700	BJ	skin:	n/a
2	chr6:167178830-167178880	HEK293	kidney:	embryo
3	chr6:167263225-167263275	ProgFib	skin:	n/a
4	chr6:167178260-167178310	PFSK-1	brain:	n/a
5	chr6:167314745-167314795	PANC-1	pancreas:	n/a
6	chr6:167189543-167189593	SK-N-SH	brain:	n/a
7	chr6:167313693-167313743	NB4	blood:	n/a
8	chr6:167313693-167313743	HNPCEpiC	eye:	n/a
9	chr6:167315653-167315703	AG04449	skin:	fetal
10	chr6:167184903-167184953	GM06990	blood:	n/a
11	chr6:167276650-167276700	BJ	skin:	n/a
12	chr6:167178830-167178880	HEK293	kidney:	embryo
13	chr6:167263225-167263275	ProgFib	skin:	n/a
14	chr6:167178260-167178310	PFSK-1	brain:	n/a
15	chr6:167314745-167314795	PANC-1	pancreas:	n/a
16	chr6:167189543-167189593	SK-N-SH	brain:	n/a
17	chr6:167313693-167313743	NB4	blood:	n/a
18	chr6:167313693-167313743	HNPCEpiC	eye:	n/a
19	chr6:167315653-167315703	AG04449	skin:	fetal
20	chr6:167184903-167184953	GM06990	blood:	n/a
21	chr6:167275684-167275734	BJ	skin:	n/a
22	chr6:167276567-167276617	HRPEpiC	eye:	n/a
23	chr6:167275395-167275445	PrEC	prostate:	n/a
24	chr6:167184903-167184953	HRPEpiC	eye:	n/a
25	chr6:167275684-167275734	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:167192573-167192623	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:167129857-167129907	Jurkat	blood:	n/a
28	chr6:167175937-167175987	ECC-1	luminal epithelium:	n/a
29	chr6:167202522-167202572	H1-hESC	embryonic stem cell:	embryo
30	chr6:167315653-167315703	NT2-D1	testis:	n/a
31	chr6:167116208-167116258	AG09319	gingival:	n/a
32	chr6:167284353-167284403	AG09309	skin:	n/a
33	chr6:167276419-167276469	GM12891	blood:	n/a
34	chr6:167276359-167276409	HAEpiC	amniotic membrane:	n/a
35	chr6:167263225-167263275	GM12892	blood:	n/a
36	chr6:167275834-167275884	ECC-1	luminal epithelium:	n/a
37	chr6:167178830-167178880	ProgFib	skin:	n/a
38	chr6:167190034-167190084	AoSMC	blood vessel:	n/a
39	chr6:167173343-167173393	AG10803	skin:	n/a
40	chr6:167136259-167136309	GM12878	blood:	n/a
41	chr6:167152254-167152304	Hela-S3	cervix:	n/a
42	chr6:167188753-167188803	T-47D	breast:	n/a
43	chr6:167275755-167275805	HRPEpiC	eye:	n/a
44	chr6:167275999-167276049	AG09309	skin:	n/a
45	chr6:167194813-167194863	AG04450	lung:	fetal
46	chr6:167314433-167314483	GM12878	blood:	n/a
47	chr6:167276275-167276325	HEK293	kidney:	embryo
48	chr6:167192488-167192538	T-47D	breast:	n/a
49	chr6:167178918-167178968	HCM	heart:	n/a
50	chr6:167190149-167190199	Jurkat	blood:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:167120732..167121236-chr6:167185691..167186290,2	MCF-7	breast:
2	chr6:167137568..167139620-chr6:167143450..167146444,3	K562	blood:
3	chr6:167200031..167200812-chr6:167555407..167555996,2	K562	blood:
4	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
5	chr6:167160489..167162374-chr6:167163032..167165986,2	K562	blood:
6	chr6:167146144..167148491-chr6:167149549..167152414,3	K562	blood:
7	chr6:167187421..167189873-chr6:167410909..167412648,3	MCF-7	breast:
8	chr6:167137568..167139295-chr6:167143450..167146444,2	K562	blood:
9	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
10	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
11	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
12	chr6:167173252..167177821-chr6:167180840..167184779,4	K562	blood:
13	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
14	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
15	chr6:167324476..167326634-chr6:167338829..167341348,2	K562	blood:
16	chr6:167327598..167330047-chr6:167367070..167369538,2	K562	blood:
17	chr6:167198453..167200233-chr6:167409946..167412844,2	K562	blood:
18	chr6:167186547..167188661-chr6:167553295..167555799,2	K562	blood:
19	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
20	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
21	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
22	chr6:167137568..167139295-chr6:167143450..167146444,2	K562	blood:
23	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
24	chr6:167327579..167329886-chr6:167332499..167334100,2	K562	blood:
25	chr6:167199917..167200852-chr6:167555354..167555927,2	MCF-7	breast:
26	chr6:167324856..167326395-chr6:167326764..167328274,2	K562	blood:
27	chr6:167187491..167191588-chr6:167191761..167196442,4	K562	blood:
28	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
29	chr6:167266120..167268418-chr6:167368019..167370456,2	K562	blood:
30	chr6:167172089..167173654-chr6:167192090..167194256,2	K562	blood:
31	chr6:167268417..167269941-chr6:167289089..167292061,2	K562	blood:
32	chr6:167339433..167341286-chr6:167346948..167348863,2	K562	blood:
33	chr6:167173631..167176313-chr6:167188907..167191189,2	K562	blood:
34	chr6:167187969..167188996-chr6:167555512..167556325,4	MCF-7	breast:
35	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
36	chr6:167334630..167336985-chr6:167348242..167350494,2	K562	blood:
37	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
38	chr6:167179347..167182239-chr6:167183994..167186208,2	K562	blood:
39	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
40	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
41	chr6:167188440..167189341-chr6:167411317..167412076,2	MCF-7	breast:
42	chr6:167327579..167329886-chr6:167332499..167334100,2	K562	blood:
43	chr6:167173631..167176313-chr6:167188907..167191189,2	K562	blood:
44	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
45	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
46	chr6:167316933..167319053-chr6:167320800..167322909,2	K562	blood:
47	chr6:167324257..167326145-chr6:167328411..167330868,2	K562	blood:
48	chr6:167324257..167326145-chr6:167328411..167330868,2	K562	blood:
49	chr6:167185783..167186302-chr6:167555369..167556350,2	K562	blood:
50	chr6:167173252..167177821-chr6:167180840..167184779,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-11	chr6:167237778-167238313	NONHSAT116055
2	lnc-FGFR1OP-1	chr6:167321422-167321647	l_3322_chr6:167314133-167321259_testes
3	lnc-FGFR1OP-1	chr6:167317186-167317276	XLOC_005539
4	lnc-FGFR1OP-1	chr6:167319514-167321259	l_3322_chr6:167314133-167321259_testes
5	lnc-RNASET2-3	chr6:167315613-167316152	NONHSAT116059
6	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes
7	lnc-RNASET2-3	chr6:167317848-167318299	NONHSAT116059
8	lnc-FGFR1OP-1	chr6:167314134-167317318	l_3322_chr6:167314133-167321259_testes
9	lnc-FGFR1OP-11	chr6:167237176-167237266	NONHSAT116055
10	lnc-FGFR1OP-10	chr6:167242352-167242576	l_3320_chr6:167242351-167255400_testes
11	lnc-FGFR1OP-1	chr6:167317788-167318323	XLOC_005539
12	lnc-FGFR1OP-1	chr6:167317788-167318557	NR_046644
13	lnc-FGFR1OP-1	chr6:167317186-167317276	NR_046644

No data

Variant related genes	Relation type
ENSG00000235008	TF binding region
RPS6KA2	TF binding region
RPS6KA2-AS1	TF binding region
ENSG00000235008	CpG island
RPS6KA2	CpG island
RPS6KA2-AS1	CpG island
ENSG00000071242	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000272980	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000197146	chromatin interactions
ENSG00000231654	chromatin interactions
ENSG00000249141	chromatin interactions
ENSG00000213066	chromatin interactions
ENSG00000227598	chromatin interactions

Extended variants
information (count: 10547 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:10547 , 50 per page) page: 1 2 3 4 5 6 7 ... 211

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181561141	chr6:167108758-167108759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370881256	chr6:167108778-167108779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147120423	chr6:167108782-167108783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148155073	chr6:167108795-167108796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545345305	chr6:167108817-167108818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527737435	chr6:167108823-167108824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73261012	chr6:167108832-167108833	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541895440	chr6:167108833-167108834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76183440	chr6:167108834-167108835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186328829	chr6:167108835-167108836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545897833	chr6:167108858-167108859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531489768	chr6:167108891-167108892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113820491	chr6:167108895-167108896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532193008	chr6:167109025-167109026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547261513	chr6:167109044-167109045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565665779	chr6:167109049-167109050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374438215	chr6:167109053-167109054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529675983	chr6:167109069-167109070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549992449	chr6:167109070-167109071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367832205	chr6:167109170-167109171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs386708507	chr6:167109199-167109200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9459717	chr6:167109200-167109201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371315843	chr6:167109219-167109220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9459718	chr6:167109224-167109225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561711462	chr6:167109238-167109239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372967462	chr6:167109241-167109242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138889117	chr6:167109257-167109258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571020733	chr6:167109262-167109263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9459719	chr6:167109267-167109268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9459720	chr6:167109268-167109269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535251430	chr6:167109276-167109277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553678641	chr6:167109281-167109282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9457195	chr6:167109286-167109287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542207132	chr6:167109294-167109295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4991784	chr6:167109295-167109296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575605777	chr6:167109313-167109314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539297219	chr6:167109314-167109315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4991783	chr6:167109319-167109320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532154299	chr6:167109324-167109325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371782842	chr6:167109333-167109334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189459446	chr6:167109352-167109353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180697481	chr6:167109360-167109361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548467413	chr6:167109362-167109363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569507553	chr6:167109363-167109364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530533679	chr6:167109364-167109365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375345376	chr6:167109371-167109372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113610697	chr6:167109379-167109380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535223481	chr6:167109390-167109391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78928076	chr6:167109437-167109438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371610847	chr6:167109442-167109443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22549408	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD

Chromatin state (count:2490 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167096800-167111600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:167102200-167116000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:167102200-167116600	Weak transcription	Brain Anterior Caudate	brain
4	chr6:167102200-167117600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:167102600-167108800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:167105600-167111400	Weak transcription	Right Atrium	heart
7	chr6:167106000-167113000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr6:167108600-167109200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:167108800-167109000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:167109200-167117000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:167109400-167111400	Enhancers	Primary B cells from peripheral blood	blood
12	chr6:167110200-167111000	Enhancers	Primary B cells from cord blood	blood
13	chr6:167110800-167111000	Enhancers	GM12878-XiMat	blood
14	chr6:167110800-167111400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:167111400-167112600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:167111600-167112800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr6:167112400-167112800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr6:167112600-167112800	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:167112600-167113800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:167112800-167115200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr6:167112800-167116600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:167113600-167115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:167113600-167115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:167114000-167114800	Enhancers	Primary hematopoietic stem cells	blood
25	chr6:167114000-167115000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr6:167115000-167115200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr6:167115000-167120800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:167115200-167115800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:167115200-167116000	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr6:167115200-167120400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:167115400-167118400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:167115800-167118000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr6:167116000-167116200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:167116000-167116400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr6:167116000-167117800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:167116000-167118000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:167116000-167118400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:167116000-167118400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr6:167116200-167116600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:167116400-167116600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:167116400-167117400	Enhancers	Fetal Brain Male	brain
42	chr6:167116400-167117800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr6:167116400-167118000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr6:167116400-167118000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr6:167116600-167116800	Enhancers	Stomach Mucosa	stomach
46	chr6:167116600-167117000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr6:167116600-167117200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr6:167116600-167117200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr6:167116600-167117200	Enhancers	Duodenum Mucosa	Duodenum
50	chr6:167116600-167117400	Enhancers	Brain Anterior Caudate	brain

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