Variant report

Variant	nsv874665
Chromosome Location	chr2:96370571-96596515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1000)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:96394384-96394976	HepG2	liver:	n/a	n/a
2	ATF1	chr2:96595249-96595443	K562	blood:	n/a	n/a
3	ATF1	chr2:96517700-96517757	K562	blood:	n/a	n/a
4	ATF1	chr2:96521076-96521271	K562	blood:	n/a	n/a
5	BACH1	chr2:96526429-96526517	K562	blood:	n/a	n/a
6	BACH1	chr2:96492683-96492753	K562	blood:	n/a	n/a
7	BATF	chr2:96491153-96491435	GM12878	blood:	n/a	n/a
8	BATF	chr2:96389586-96389891	GM12878	blood:	n/a	n/a
9	BATF	chr2:96533155-96533370	GM12878	blood:	n/a	n/a
10	BATF	chr2:96373042-96373284	GM12878	blood:	n/a	chr2:96373152-96373163
11	BATF	chr2:96389629-96389835	GM12878	blood:	n/a	n/a
12	BATF	chr2:96373017-96373229	GM12878	blood:	n/a	chr2:96373152-96373163
13	BATF	chr2:96401104-96401456	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:96442951-96443157	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:96401104-96401290	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:96594562-96594761	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:96401015-96401259	GM12878	blood:	n/a	n/a
18	BCL3	chr2:96468045-96468276	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:96394763-96394892	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:96557498-96557706	HepG2	liver:	n/a	n/a
21	BHLHE40	chr2:96533093-96533344	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:96526629-96526661	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:96577237-96577420	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:96432533-96432779	K562	blood:	n/a	n/a
25	CEBPB	chr2:96479121-96479321	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:96394271-96395330	HepG2	liver:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
27	CEBPB	chr2:96576685-96576797	A549	lung:	n/a	n/a
28	CEBPB	chr2:96426939-96427088	HepG2	liver:	n/a	chr2:96427040-96427051
29	CEBPB	chr2:96391404-96391735	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:96577216-96577553	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:96394709-96395335	K562	blood:	n/a	n/a
32	CEBPB	chr2:96426837-96427246	IMR90	lung:	n/a	chr2:96427040-96427051
33	CEBPB	chr2:96394289-96395327	IMR90	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
34	CEBPB	chr2:96482692-96482778	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:96394342-96395320	A549	lung:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
36	CEBPB	chr2:96482679-96482785	A549	lung:	n/a	n/a
37	CEBPB	chr2:96504906-96504952	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:96556161-96556364	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:96556081-96556287	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:96394654-96395269	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:96394684-96394919	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:96556160-96556378	A549	lung:	n/a	n/a
43	CEBPB	chr2:96394316-96394473	K562	blood:	n/a	chr2:96394419-96394430 chr2:96394419-96394432
44	CEBPB	chr2:96426902-96427182	MCF-7	breast:	n/a	chr2:96427040-96427051
45	CEBPB	chr2:96426884-96427208	Hela-S3	cervix:	n/a	chr2:96427040-96427051
46	CHD2	chr2:96577302-96577508	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr2:96395040-96395190	AG09319	gingival:	n/a	n/a
48	CTCF	chr2:96440944-96441098	GM12891	blood:	n/a	n/a
49	CTCF	chr2:96429789-96429903	GM13976	blood:	n/a	chr2:96429822-96429840
50	CTCF	chr2:96456128-96456210	Lung_OC	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96458247-96458297	HNPCEpiC	eye:	n/a
2	chr2:96458247-96458297	GM12878	blood:	n/a
3	chr2:96427173-96427223	Hela-S3	cervix:	n/a
4	chr2:96458247-96458297	NT2-D1	testis:	n/a
5	chr2:96427173-96427223	HEEpiC	esophagus:	n/a
6	chr2:96458247-96458297	A549	lung:	n/a
7	chr2:96427173-96427223	ProgFib	skin:	n/a
8	chr2:96458247-96458297	HCM	heart:	n/a
9	chr2:96427173-96427223	LNCaP	prostate:	n/a
10	chr2:96427173-96427223	NH-A	brain:	n/a
11	chr2:96458247-96458297	Jurkat	blood:	n/a
12	chr2:96458247-96458297	NHDF-neo	bronchial:	n/a
13	chr2:96427173-96427223	Caco-2	colon:	n/a
14	chr2:96458247-96458297	NHBE	bronchial:	n/a
15	chr2:96458247-96458297	PANC-1	pancreas:	n/a
16	chr2:96458247-96458297	H1-hESC	embryonic stem cell:	embryo
17	chr2:96458247-96458297	HCPEpiC	choroid plexus:	n/a
18	chr2:96458247-96458297	IMR90	lung:	fetal
19	chr2:96427173-96427223	IMR90	lung:	fetal
20	chr2:96427173-96427223	T-47D	breast:	n/a
21	chr2:96427173-96427223	HMEC	breast:	n/a
22	chr2:96427173-96427223	HRPEpiC	eye:	n/a
23	chr2:96458247-96458297	RPTEC	kidney:	n/a
24	chr2:96458247-96458297	NB4	blood:	n/a
25	chr2:96427173-96427223	PrEC	prostate:	n/a
26	chr2:96427173-96427223	RPTEC	kidney:	n/a
27	chr2:96458247-96458297	K562	blood:	n/a
28	chr2:96427173-96427223	HNPCEpiC	eye:	n/a
29	chr2:96458247-96458297	HEK293	kidney:	embryo
30	chr2:96458247-96458297	HUVEC	blood vessel:	n/a
31	chr2:96458247-96458297	SK-N-SH_RA	brain:	n/a
32	chr2:96427173-96427223	AG09309	skin:	n/a
33	chr2:96427173-96427223	ECC-1	luminal epithelium:	n/a
34	chr2:96458247-96458297	MCF10A-Er-Src	breast:	n/a
35	chr2:96427173-96427223	HAEpiC	amniotic membrane:	n/a
36	chr2:96458247-96458297	PFSK-1	brain:	n/a
37	chr2:96458247-96458297	SK-N-SH	brain:	n/a
38	chr2:96427173-96427223	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:96427173-96427223	PFSK-1	brain:	n/a
40	chr2:96427173-96427223	NT2-D1	testis:	n/a
41	chr2:96458247-96458297	T-47D	breast:	n/a
42	chr2:96427173-96427223	SK-N-MC	brain:	n/a
43	chr2:96458247-96458297	Caco-2	colon:	n/a
44	chr2:96427173-96427223	HIPEpiC	eye:	n/a
45	chr2:96427173-96427223	BE2_C	brain:	n/a
46	chr2:96427173-96427223	AG04450	lung:	fetal
47	chr2:96458247-96458297	LNCaP	prostate:	n/a
48	chr2:96458247-96458297	HCF	heart:	n/a
49	chr2:96427173-96427223	GM12891	blood:	n/a
50	chr2:96458247-96458297	AoSMC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:96406055..96406842-chr2:114139694..114140465,2	MCF-7	breast:
2	chr13:60970490..60971024-chr2:96378837..96379342,2	NB4	blood:
3	chr2:96054886..96055732-chr2:96394556..96395496,2	MCF-7	breast:
4	chr2:96054634..96055511-chr2:96394406..96395211,2	MCF-7	breast:
5	chr2:96079865..96080377-chr2:96394455..96395330,2	K562	blood:
6	chr2:96011050..96011912-chr2:96394384..96395342,2	MCF-7	breast:
7	chr2:96058513..96059040-chr2:96394487..96395166,2	MCF-7	breast:
8	chr2:96054639..96055198-chr2:96394784..96395584,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36C-2	chr2:96383793-96384234	XLOC_002206
2	lnc-GPAT2-6	chr2:96533188-96533219	NONHSAT072520
3	lnc-ANKRD36C-1	chr2:96472866-96473050	ENSG00000232931
4	lnc-TRIM43-2	chr2:96477742-96477871	XLOC_001576
5	lnc-GPAT2-6	chr2:96525609-96525822	NONHSAT072520
6	lnc-ANKRD36C-1	chr2:96472800-96473050	NONHSAT072509
7	lnc-TRIM43-2	chr2:96479687-96479710	NONHSAT072515
8	lnc-ANKRD36C-2	chr2:96379286-96379320	XLOC_002206
9	lnc-ANKRD36C-1	chr2:96472813-96473050	NONHSAT072510
10	lnc-ANKRD36C-1	chr2:96479798-96482417	NONHSAT072514
11	lnc-ANKRD36C-1	chr2:96479174-96479284	NONHSAT072514
12	lnc-GPAT2-5	chr2:96557405-96557647	ucscGeneNc_uc002swd_1
13	lnc-ANKRD36C-1	chr2:96479079-96479705	NONHSAT072513
14	lnc-ANKRD36C-1	chr2:96479657-96479705	ENSG00000232931
15	lnc-ANKRD36C-1	chr2:96489949-96492729	NONHSAT072509
16	lnc-TRIM43-2	chr2:96479803-96480574	NONHSAT072515
17	lnc-GPAT2-5	chr2:96561691-96561770	ucscGeneNc_uc002swd_1
18	lnc-TRIM43-2	chr2:96479581-96479705	XLOC_001576
19	lnc-ANKRD36C-1	chr2:96480419-96480840	NONHSAT072516
20	lnc-ANKRD36C-1	chr2:96479064-96479281	ENSG00000232931
21	lnc-ANKRD36C-1	chr2:96479558-96479705	NONHSAT072514
22	lnc-ANKRD36C-1	chr2:96479798-96482510	NONHSAT072510
23	lnc-ANKRD36C-1	chr2:96479798-96486944	NONHSAT072513
24	lnc-GPAT2-5	chr2:96559198-96559313	ucscGeneNc_uc002swd_1
25	lnc-ANKRD36C-1	chr2:96479810-96479882	NONHSAT072516
26	lnc-GPAT2-6	chr2:96523088-96523240	NONHSAT072520
27	lnc-ANKRD36C-1	chr2:96479798-96479893	ENSG00000232931
28	lnc-ANKRD36C-1	chr2:96480419-96480524	ENSG00000232931
29	lnc-ANKRD36C-1	chr2:96479798-96479893	NONHSAT072509

No data

Variant related genes	Relation type
ENSG00000237510	TF binding region
LINC00342	TF binding region
ANKRD36C	TF binding region
ENSG00000237510	CpG island
LINC00342	CpG island
ANKRD36C	CpG island
ENSG00000083544	chromatin interactions
ENSG00000248821	chromatin interactions
SACS	miRNA target sites
KIF23	miRNA target sites

Extended variants
information (count: 6246 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:6246 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11676901	chr2:96370571-96370572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541159180	chr2:96370631-96370632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184041801	chr2:96370645-96370646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577862861	chr2:96370679-96370680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543643324	chr2:96370750-96370751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564018015	chr2:96370788-96370789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529516025	chr2:96370808-96370809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189943500	chr2:96370850-96370851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192163169	chr2:96370889-96370890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145368233	chr2:96370904-96370905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559082384	chr2:96370905-96370906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533001497	chr2:96370920-96370921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184424096	chr2:96370943-96370944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76652729	chr2:96370966-96370967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547545301	chr2:96370992-96370993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71981663	chr2:96371067-96371068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs57291054	chr2:96371076-96371077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61426802	chr2:96371077-96371078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570561289	chr2:96371078-96371079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533195843	chr2:96371097-96371098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374914198	chr2:96371153-96371154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189354323	chr2:96371162-96371163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552251438	chr2:96371222-96371223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181804251	chr2:96371237-96371238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535352009	chr2:96371293-96371294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555617884	chr2:96371311-96371312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565764346	chr2:96371322-96371323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534695283	chr2:96371365-96371366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557869912	chr2:96371403-96371404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577673793	chr2:96371480-96371481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186404578	chr2:96371544-96371545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570950638	chr2:96371547-96371548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537834382	chr2:96371575-96371576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557247253	chr2:96371591-96371592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72821452	chr2:96371641-96371642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs367575516	chr2:96371698-96371699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542986151	chr2:96371722-96371723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544933387	chr2:96371892-96371893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188800176	chr2:96371914-96371915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560070019	chr2:96371952-96371953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527331209	chr2:96372076-96372077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181608339	chr2:96372089-96372090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186162774	chr2:96372160-96372161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113969296	chr2:96372173-96372174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145159621	chr2:96372174-96372175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371413864	chr2:96372259-96372260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549962950	chr2:96372269-96372270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568380879	chr2:96372270-96372271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569782635	chr2:96372304-96372305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529059927	chr2:96372324-96372325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96361600-96374600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:96374600-96374800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:96374600-96375000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:96374800-96375800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:96375000-96384600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:96375800-96377200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:96377000-96377200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:96377200-96379000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:96377200-96379000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:96378200-96381600	Enhancers	Fetal Lung	lung
11	chr2:96378600-96379000	Enhancers	Fetal Kidney	kidney
12	chr2:96378600-96380000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:96378800-96379200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:96378800-96379200	Enhancers	Duodenum Mucosa	Duodenum
15	chr2:96378800-96380200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:96378800-96380600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:96379000-96380000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:96379000-96380200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:96379200-96379600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr2:96379200-96380000	Enhancers	Primary hematopoietic stem cells	blood
21	chr2:96379200-96380400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:96379200-96380400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:96379200-96380600	Enhancers	Fetal Intestine Large	intestine
24	chr2:96379200-96380600	Enhancers	Fetal Intestine Small	intestine
25	chr2:96379400-96380000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr2:96379400-96380000	Enhancers	Fetal Stomach	stomach
27	chr2:96379400-96380200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr2:96379400-96380200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:96379600-96380000	Enhancers	Small Intestine	intestine
30	chr2:96379600-96380400	Enhancers	Duodenum Mucosa	Duodenum
31	chr2:96379800-96380200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:96380000-96384800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:96381600-96385800	Weak transcription	Fetal Lung	lung
34	chr2:96384600-96386200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:96384800-96385400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:96384800-96386000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:96385400-96386000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr2:96385800-96386000	Enhancers	Fetal Lung	lung
39	chr2:96385800-96386000	Enhancers	Gastric	stomach
40	chr2:96385800-96386000	Enhancers	Stomach Smooth Muscle	stomach
41	chr2:96386000-96386600	Enhancers	Lung	lung
42	chr2:96386200-96387400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:96387800-96388000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:96391000-96391800	Enhancers	NHDF-Ad	bronchial
45	chr2:96391800-96394400	Weak transcription	NHDF-Ad	bronchial
46	chr2:96392800-96395200	Enhancers	Liver	Liver
47	chr2:96394400-96394600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:96394400-96394800	Enhancers	Fetal Stomach	stomach
49	chr2:96394400-96394800	Enhancers	HSMM	muscle
50	chr2:96394600-96394800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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