Variant report

Variant	nsv830410
Chromosome Location	chr5:95505799-95666310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1867)
CpG islands
(count:793)
Chromatin interactive
region (count:21)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1867 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95523195-95523769	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:95531796-95532242	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:95610841-95611188	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:95633109-95634238	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:95535336-95536476	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:95581064-95581603	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:95562820-95563009	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:95624520-95624890	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:95550628-95550982	HepG2	liver:	n/a	n/a
10	ATF1	chr5:95592601-95592850	K562	blood:	n/a	n/a
11	ATF1	chr5:95628373-95628550	K562	blood:	n/a	n/a
12	ATF1	chr5:95515236-95515349	K562	blood:	n/a	n/a
13	ATF2	chr5:95556405-95556814	GM12878	blood:	n/a	n/a
14	ATF2	chr5:95556378-95556814	GM12878	blood:	n/a	n/a
15	ATF2	chr5:95662466-95663031	GM12878	blood:	n/a	n/a
16	ATF2	chr5:95615490-95616387	GM12878	blood:	n/a	n/a
17	ATF2	chr5:95662435-95663079	GM12878	blood:	n/a	n/a
18	ATF2	chr5:95513034-95513668	GM12878	blood:	n/a	n/a
19	ATF2	chr5:95512965-95513671	GM12878	blood:	n/a	n/a
20	ATF2	chr5:95615601-95616391	GM12878	blood:	n/a	n/a
21	BACH1	chr5:95593572-95593815	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr5:95594980-95595488	K562	blood:	n/a	chr5:95595120-95595134
23	BACH1	chr5:95594913-95595343	H1-hESC	embryonic stem cell:	n/a	chr5:95595120-95595134
24	BACH1	chr5:95596621-95596733	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr5:95592619-95592751	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr5:95546561-95546757	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr5:95615461-95616313	GM12878	blood:	n/a	n/a
28	BATF	chr5:95662627-95662962	GM12878	blood:	n/a	n/a
29	BATF	chr5:95513032-95513607	GM12878	blood:	n/a	chr5:95513318-95513329
30	BATF	chr5:95556408-95556754	GM12878	blood:	n/a	chr5:95556552-95556563
31	BATF	chr5:95513119-95513616	GM12878	blood:	n/a	chr5:95513318-95513329
32	BATF	chr5:95615818-95616321	GM12878	blood:	n/a	n/a
33	BATF	chr5:95564194-95564485	GM12878	blood:	n/a	chr5:95564355-95564366
34	BATF	chr5:95623947-95624227	GM12878	blood:	n/a	chr5:95624001-95624009
35	BATF	chr5:95662556-95662996	GM12878	blood:	n/a	n/a
36	BATF	chr5:95633559-95633773	GM12878	blood:	n/a	chr5:95633605-95633614
37	BATF	chr5:95556266-95556804	GM12878	blood:	n/a	chr5:95556552-95556563
38	BCL11A	chr5:95513024-95513657	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:95662602-95662985	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:95615563-95616330	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:95615908-95616193	GM12878	blood:	n/a	n/a
42	BCL11A	chr5:95564243-95564493	GM12878	blood:	n/a	chr5:95564355-95564364
43	BCL11A	chr5:95556405-95556726	GM12878	blood:	n/a	n/a
44	BCL3	chr5:95615883-95616323	GM12878	blood:	n/a	n/a
45	BCL3	chr5:95590615-95591173	A549	lung:	n/a	chr5:95590792-95590801 chr5:95590791-95590800
46	BCL3	chr5:95513115-95513601	GM12878	blood:	n/a	n/a
47	BCL3	chr5:95581015-95581512	A549	lung:	n/a	n/a
48	BCL3	chr5:95590537-95591423	A549	lung:	n/a	chr5:95590792-95590801 chr5:95590791-95590800
49	BCL3	chr5:95662573-95662945	GM12878	blood:	n/a	n/a
50	BCLAF1	chr5:95513016-95513698	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95651711-95651761	AoSMC	blood vessel:	n/a
2	chr5:95553592-95553642	PFSK-1	brain:	n/a
3	chr5:95590917-95590967	HRE	kidney:	n/a
4	chr5:95562504-95562554	ProgFib	skin:	n/a
5	chr5:95555970-95556020	Hepatocyte	liver:	n/a
6	chr5:95509647-95509697	GM06990	blood:	n/a
7	chr5:95571107-95571157	HNPCEpiC	eye:	n/a
8	chr5:95659536-95659586	NH-A	brain:	n/a
9	chr5:95666291-95666341	BJ	skin:	n/a
10	chr5:95514729-95514779	HCM	heart:	n/a
11	chr5:95555970-95556020	BE2_C	brain:	n/a
12	chr5:95555970-95556020	SAEC	small airway:	n/a
13	chr5:95666291-95666341	SKMC	muscle:	n/a
14	chr5:95514729-95514779	NH-A	brain:	n/a
15	chr5:95555970-95556020	SK-N-SH	brain:	n/a
16	chr5:95553592-95553642	MCF10A-Er-Src	breast:	n/a
17	chr5:95509647-95509697	BE2_C	brain:	n/a
18	chr5:95555970-95556020	Caco-2	colon:	n/a
19	chr5:95571107-95571157	HRPEpiC	eye:	n/a
20	chr5:95553592-95553642	Caco-2	colon:	n/a
21	chr5:95659536-95659586	BE2_C	brain:	n/a
22	chr5:95514729-95514779	GM12891	blood:	n/a
23	chr5:95590917-95590967	BJ	skin:	n/a
24	chr5:95571107-95571157	HMEC	breast:	n/a
25	chr5:95634103-95634153	HMEC	breast:	n/a
26	chr5:95666291-95666341	HCM	heart:	n/a
27	chr5:95562504-95562554	HepG2	liver:	n/a
28	chr5:95583220-95583270	HCT-116	colon:	n/a
29	chr5:95666291-95666341	NHBE	bronchial:	n/a
30	chr5:95562504-95562554	AG09319	gingival:	n/a
31	chr5:95580517-95580567	HCF	heart:	n/a
32	chr5:95666291-95666341	CMK	blood:	n/a
33	chr5:95583220-95583270	HCF	heart:	n/a
34	chr5:95562504-95562554	HUVEC	blood vessel:	n/a
35	chr5:95590917-95590967	SKMC	muscle:	n/a
36	chr5:95590917-95590967	GM12891	blood:	n/a
37	chr5:95571107-95571157	HCF	heart:	n/a
38	chr5:95634103-95634153	NH-A	brain:	n/a
39	chr5:95590917-95590967	GM12878	blood:	n/a
40	chr5:95590917-95590967	AG09319	gingival:	n/a
41	chr5:95634103-95634153	Hepatocyte	liver:	n/a
42	chr5:95553592-95553642	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:95583220-95583270	SK-N-MC	brain:	n/a
44	chr5:95583220-95583270	PFSK-1	brain:	n/a
45	chr5:95583220-95583270	Caco-2	colon:	n/a
46	chr5:95509647-95509697	HEEpiC	esophagus:	n/a
47	chr5:95571107-95571157	AG09309	skin:	n/a
48	chr5:95553592-95553642	HCT-116	colon:	n/a
49	chr5:95634103-95634153	T-47D	breast:	n/a
50	chr5:95634103-95634153	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:95525860..95527522-chr5:95528640..95530648,2	K562	blood:
2	chr5:95594080..95595796-chr5:95600071..95601764,2	MCF-7	breast:
3	chr5:95595479..95598256-chr5:95600946..95602576,2	K562	blood:
4	chr5:95595479..95598256-chr5:95600946..95602576,2	K562	blood:
5	chr5:95559323..95562073-chr5:95563803..95565354,2	K562	blood:
6	chr5:95650274..95652042-chr5:95666780..95669521,2	K562	blood:
7	chr5:95514396..95516278-chr5:95516334..95518457,2	MCF-7	breast:
8	chr5:95296142..95297757-chr5:95548308..95551059,2	MCF-7	breast:
9	chr5:95621284..95624272-chr5:95627637..95629597,2	K562	blood:
10	chr5:95592206..95593260-chr5:95671508..95672757,3	MCF-7	breast:
11	chr5:95594080..95595796-chr5:95600071..95601764,2	MCF-7	breast:
12	chr5:95297197..95300138-chr5:95621802..95624032,2	K562	blood:
13	chr5:95588143..95588958-chr9:139052512..139053354,2	Hela-S3	cervix:
14	chr5:95621284..95624272-chr5:95627637..95629597,2	K562	blood:
15	chr5:95562010..95564635-chr5:95566152..95567653,2	K562	blood:
16	chr5:95525860..95527522-chr5:95528640..95530648,2	K562	blood:
17	chr5:95295813..95297730-chr5:95509691..95513158,3	MCF-7	breast:
18	chr5:95562010..95564635-chr5:95566152..95567653,2	K562	blood:
19	chr5:95514396..95516278-chr5:95516334..95518457,2	MCF-7	breast:
20	chr5:95559323..95562073-chr5:95563803..95565354,2	K562	blood:
21	chr5:95295913..95298575-chr5:95662925..95666716,4	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAST-4	chr5:95654177-95654248	ENSG00000251314.1
2	lnc-PCSK1-1	chr5:95549050-95549493	XLOC_004933
3	lnc-PCSK1-4	chr5:95666245-95666687	NONHSAT102889
4	lnc-CAST-4	chr5:95654177-95654248	ENSG00000251314.2
5	lnc-C5orf27-3	chr5:95550679-95551223	ENSG00000250551
6	lnc-CAST-4	chr5:95654177-95654722	ENSG00000251314.1
7	lnc-CAST-4	chr5:95644428-95644586	ENSG00000251314.1
8	lnc-PCSK1-1	chr5:95545140-95549493	NONHSAT102885
9	lnc-PCSK1-1	chr5:95550572-95550869	NONHSAT102885
10	lnc-CAST-4	chr5:95644428-95644586	ENSG00000251314.2
11	lnc-CAST-3	chr5:95614292-95614455	XLOC_004479
12	lnc-PCSK1-1	chr5:95550572-95550779	XLOC_004933
13	lnc-CAST-10	chr5:95546905-95548572	NONHSAT102887
14	lnc-CAST-3	chr5:95583480-95583721	XLOC_004479

No data

Variant related genes	Relation type
RNU6-524P	TF binding region
ENSG00000249746	TF binding region
ENSG00000250158	TF binding region
RNU6-524P	CpG island
ENSG00000249746	CpG island
ENSG00000250158	CpG island
ENSG00000118985	chromatin interactions
ENSG00000251314	chromatin interactions

Extended variants
information (count: 5558 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5558 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370987247	chr5:95505800-95505801	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535748732	chr5:95505807-95505808	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186767308	chr5:95505813-95505814	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541641237	chr5:95505818-95505819	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575449194	chr5:95505837-95505838	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544463948	chr5:95505841-95505842	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145147134	chr5:95505851-95505852	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578032546	chr5:95505861-95505862	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540664634	chr5:95505863-95505864	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558677199	chr5:95505869-95505870	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560297194	chr5:95505885-95505886	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115825507	chr5:95505963-95505964	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116221691	chr5:95505978-95505979	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192813351	chr5:95505996-95505997	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149142718	chr5:95506004-95506005	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551281957	chr5:95506073-95506074	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12519062	chr5:95506086-95506087	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs113045564	chr5:95506096-95506097	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371629800	chr5:95506174-95506175	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368217412	chr5:95506219-95506220	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184563091	chr5:95506232-95506233	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566945539	chr5:95506244-95506245	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61091984	chr5:95506260-95506261	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535817698	chr5:95506268-95506269	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555667961	chr5:95506269-95506270	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569191559	chr5:95506282-95506283	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189882489	chr5:95506287-95506288	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11135447	chr5:95506305-95506306	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs578087207	chr5:95506307-95506308	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192837433	chr5:95506329-95506330	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373982040	chr5:95506354-95506355	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370663581	chr5:95506363-95506364	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184414963	chr5:95506386-95506387	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189043861	chr5:95506400-95506401	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181826927	chr5:95506436-95506437	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543031248	chr5:95506461-95506462	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368136869	chr5:95506466-95506467	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139380828	chr5:95506477-95506478	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531635814	chr5:95506536-95506537	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545243859	chr5:95506555-95506556	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564943039	chr5:95506576-95506577	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574382023	chr5:95506653-95506654	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186425099	chr5:95506661-95506662	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547196812	chr5:95506673-95506674	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560628192	chr5:95506686-95506687	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554888982	chr5:95506703-95506704	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141736044	chr5:95506727-95506728	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147099349	chr5:95506728-95506729	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538157649	chr5:95506730-95506731	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552008220	chr5:95506746-95506747	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95486800-95506400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:95494000-95511600	Weak transcription	Fetal Intestine Small	intestine
3	chr5:95495000-95508000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:95495000-95508000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:95502800-95505800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:95504800-95507800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:95505800-95506800	Enhancers	Liver	Liver
8	chr5:95505800-95507800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:95506400-95507800	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr5:95506600-95506800	Active TSS	Duodenum Mucosa	Duodenum
11	chr5:95506800-95507000	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr5:95506800-95512000	Weak transcription	Liver	Liver
13	chr5:95507200-95510200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:95507400-95507600	Enhancers	Placenta Amnion	Placenta Amnion
15	chr5:95507400-95508600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:95507600-95508400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:95507800-95508000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:95507800-95508600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr5:95507800-95511200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:95508000-95508800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr5:95508000-95508800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:95508000-95508800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:95508000-95509000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:95508000-95509000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:95508000-95509000	Enhancers	HSMM	muscle
26	chr5:95508000-95509000	Enhancers	HSMMtube	muscle
27	chr5:95508000-95509000	Enhancers	NH-A	brain
28	chr5:95508000-95509000	Enhancers	Osteobl	bone
29	chr5:95508000-95509200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:95508200-95508600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:95508200-95508600	Enhancers	NHEK	skin
32	chr5:95508200-95508800	Enhancers	HMEC	breast
33	chr5:95508200-95509000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr5:95508200-95509000	Enhancers	NHDF-Ad	bronchial
35	chr5:95508400-95508600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:95508400-95508800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:95508400-95509000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr5:95508400-95509200	Enhancers	NHLF	lung
39	chr5:95508600-95509000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:95508600-95509000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr5:95508600-95511000	Weak transcription	NHEK	skin
42	chr5:95508600-95511200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:95508600-95515200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr5:95508800-95511000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:95508800-95511200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:95508800-95511200	Weak transcription	HMEC	breast
47	chr5:95508800-95512000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:95508800-95512200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:95509000-95509200	Enhancers	Fetal Lung	lung
50	chr5:95509000-95511200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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